viernes, 5 de octubre de 2018

New Reassortant Clade 2.3.4.4b Avian Influenza A(H5N6) Virus in Wild Birds, South Korea, 2017–18 - Volume 24, Number 10—October 2018 - Emerging Infectious Diseases journal - CDC

New Reassortant Clade 2.3.4.4b Avian Influenza A(H5N6) Virus in Wild Birds, South Korea, 2017–18 - Volume 24, Number 10—October 2018 - Emerging Infectious Diseases journal - CDC





Volume 24, Number 10—October 2018

Research Letter

New Reassortant Clade 2.3.4.4b Avian Influenza A(H5N6) Virus in Wild Birds, South Korea, 2017–18

Jung-Hoon Kwon1, Sol Jeong1, Dong-Hun Lee, David E. Swayne, Yu-jin Kim, Sun-hak Lee, Jin-Yong Noh, Tseren-Ochir Erdene-Ochir, Jei-Hyun Jeong, and Chang-Seon SongComments to Author 
Author affiliations: Konkuk University, Seoul, South Korea (J.-H. Kwon, S. Jeong, Y.-J. Kim, S.-H. Lee, J.-Y. Noh, T.-O. Erdene-Ochir, J.-H. Jeong, C.-S. Song)US Department of Agriculture, Athens, Georgia, USA (D.-H. Lee, D.E. Swayne)

Abstract

We isolated new reassortant avian influenza A(H5N6) viruses from feces of wild waterfowl in South Korea during 2017–18. Phylogenetic analysis suggested that reassortment occurred between clade 2.3.4.4b H5N8 and Eurasian low pathogenicity avian influenza viruses circulating in wild birds. Dissemination to South Korea during the 2017 fall migratory season followed.
Clade 2.3.4.4 H5 highly pathogenic avian influenza viruses (HPAIVs) have evolved by reassortment with different neuraminidase (NA) and internal genes of prevailing low pathogenicity avian influenza viruses (LPAIVs) and other HPAIVs to generate new genotypes and further evolved into genetic subgroups A–D since 2014 (1). Among these, subgroups A and B viruses were disseminated over vast geographic regions by migratory wild birds (2,3). Subgroup B influenza A(H5N8) viruses were detected in Qinghai Lake, China, and Uvs-Nuur Lake, Russia, during May–June 2016 (Qinghai/Uvs-like), followed by the identification of reassortant viruses in multiple Eurasian countries (46). Recently, subgroup B H5N6 viruses were isolated from birds in Greece during February 2017 and England, Germany, the Netherlands, Japan, and Taiwan during winter 2017–18 (7,8).
During December 2017–January 2018 in South Korea, we isolated 6 H5N6 HPAIVs from 231 fecal samples of wild birds collected from the banks of the Cheongmi-cheon River (37°06′56.9′′N, 127°25′18.3′′E) and 34 from 222 fecal samples collected from the banks of the Gokgyo-cheon River (36°45′12.3″N, 127°07′12.7″E) (Technical Appendix 1). These wild bird habitats are wintering sites of migratory waterfowl, including mallard (Anas platyrhynchos), spot-billed duck (Anas poecilorhyncha), Mandarin duck (Aix galericulata), and common teal (Anas crecca). The Gokgyo-cheon River is a major habitat site for Mandarin ducks, and numerous HPAIVs were detected in fecal samples from Mandarin ducks during 2011, 2015, and 2016 (9). We identified avian influenza virus–positive fecal samples from 38 Mandarin ducks and 2 mallards, based on DNA barcoding technique (10). We performed full-length genome sequencing and comparative phylogenetic analysis on 19 of the 40 isolates (Technical Appendix 1Technical Appendix 2).
All H5N6 isolates shared high nucleotide sequence identities in all 8 gene segments (99.58%–100%) and were identified as HPAIVs based on the presence of multiple basic amino acids at the HA proteolytic cleavage site (PLREKRRKR/G). Searches of the GISAID (https://www.gisaid.org) and BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi) databases indicated that all 8 genomes had the highest nucleotide identity with A/Great_Black-backed_Gull/Netherlands/1/2017 (Netherlands/1) clade 2.3.4.4 subgroup B H5N6 strain from December 2017 (99.17%–99.79%), rather than subgroup B H5N6 viruses from Japan and Taiwan collected during December 2017 (97.18%–99.27%).
In phylogenetic analysis, we identified 2 genotypes of subgroup B H5N6 viruses (Technical Appendix 1 Figures 1, 2): genotypes B.N6.1 and B.N6.2. The genotype B.N6.1 viruses were identified from South Korea, Japan, Taiwan, Greece, and the Netherlands (Netherlands/1 strain), and the genotype B.N6.2 viruses were detected from England, Germany, and the Netherlands. For genotype B.N6.1, all genes except NA clustered with H5N8 HPAIV of previously reported genotypes, H5N8-NL cluster I in the Netherlands (6), Ger-11-16 in Germany (5), and Duck/Poland/82a/16-like in Italy (4). The NA gene clustered with LPAIVs circulating in wild birds in Eurasia and separated into 2 clusters, suggesting the potential for >2 independent reassortment events between H5N8 virus and unidentified wild bird origin N6 segments. Consistent clustering of South Korea isolates with the Netherlands/1 strain in maximum-likelihood (ML) phylogenies for each gene supported by high ML bootstrap values (86–100) suggests their close relationship. The genotype B.N6.2 viruses had different polymerase basic 2 (PB2) and polymerase acidic (PA) genes from genotype B.N6.1. The polymerase basic 2 gene probably originated from other LPAIVs, and a polymerase acidic gene originated from H5N8-NL cluster II genotype (6,7). The phylogenetic network and ML analysis suggest that H5N6 viruses have evolved from subgroup B H5N8 viruses into 3 independent pathways, detected in Greece, Europe/South Korea, and Japan/Taiwan (Technical Appendix 1 Figures 2, 3).
The time of most recent common ancestry (tMRCA) for each gene of genotype B.N6.1 H5N6 viruses isolated during winter 2017–18 in Eurasia, except for the NA gene, ranged from January 2016 to October 2016, suggesting that genotype B.N6.1 viruses diverged during the previous year. The tMRCA of the NA gene was September 2015 (95% highest posterior density August 2014–August 2016). The tMRCA of the NA gene has wide 95% highest posterior density range because only a few recent N6 genes of LPAIVs were available in databases for analysis. The tMRCA for each gene of H5N6 HPAIVs identified in South Korea ranged from July through September 2017, suggesting that ancestors of these viruses emerged among wild birds during or after summer 2017, possibly at the breeding and molting sites in the Palearctic region (TableTechnical Appendix 1 Figure 4). Detection of H5N6 HPAIV from fecal samples of wild birds in South Korea during the 2017–18 wintering season and our phylogenetic analysis suggest that the viruses had moved through wild birds during the fall migration season.
On the basis of our data and migratory pattern of birds, we estimate that H5N6 viruses possibly descended from H5N8 viruses circulating during 2016–17, reaching breeding regions of wild birds during early 2017, followed by dissemination into Europe and East Asia during the fall migration. Enhanced surveillance in wild birds is needed for early detection of new introductions of HPAIV and to trace the transmission route of HPAIV.
Mr. Kwon is a PhD candidate at Konkuk University, Seoul, South Korea. His primary research interest is the epidemiology of HPAIVs in wild birds. Ms. Jeong is a PhD candidate at Konkuk University, Seoul. Her primary research interest is the epidemiology of viruses in wild birds.
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Acknowledgment

This work was funded by Konkuk University in 2015.
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References

  1. Sonnberg  SWebby  RJWebster  RGNatural history of highly pathogenic avian influenza H5N1. Virus Res2013;178:6377DOIPubMed
  2. Lee  DHBertran  KKwon  JHSwayne  DEEvolution, global spread, and pathogenicity of highly pathogenic avian influenza H5Nx clade 2.3.4.4. J Vet Sci2017;18(S1):26980DOIPubMed
  3. Global Consortium for H5N8 and Related Influenza VirusesRole for migratory wild birds in the global spread of avian influenza H5N8. Science2016;354:2137DOIPubMed
  4. Fusaro  AMonne  IMulatti  PZecchin  BBonfanti  LOrmelli  Set al. Genetic diversity of highly pathogenic avian influenza A(H5N8/H5N5) viruses in Italy, 2016–17. Emerg Infect Dis2017;23:15437DOIPubMed
  5. Pohlmann  AStarick  EGrund  CHöper  DStrebelow  GGlobig  Aet al. Swarm incursions of reassortants of highly pathogenic avian influenza virus strains H5N8 and H5N5, clade 2.3.4.4b, Germany, winter 2016/17. Sci Rep2018;8:15DOIPubMed
  6. Beerens  NHeutink  RBergervoet  SAHarders  FBossers  AKoch  GMultiple reassorted viruses as cause of highly pathogenic avian influenza A(H5N8) virus epidemic, the Netherlands, 2016. Emerg Infect Dis2017;23:197481DOIPubMed
  7. Beerens  NKoch  GHeutink  RHarders  FVries  DPEHo  Cet al. Novel highly pathogenic avian influenza A(H5N6) virus in the Netherlands, December 2017. Emerg Infect Dis2018;24:7703DOIPubMed
  8. Liu  YPLee  DHChen  LHLin  YJLi  WCHu  SCet al. Detection of reassortant H5N6 clade 2.3.4.4 highly pathogenic avian influenza virus in a black-faced spoonbill (Platalea minor) found dead, Taiwan, 2017. Infect Genet Evol2018;62:2758DOIPubMed
  9. Kwon  JHLee  DHSwayne  DENoh  JYYuk  SSErdene-Ochir  TOet al. Reassortant clade 2.3.4.4 avian influenza A(H5N6) virus in a wild Mandarin duck, South Korea, 2016. Emerg Infect Dis2017;23:8226DOIPubMed
  10. Lee  DHLee  HJLee  YJKang  HMJeong  OMKim  MCet al. DNA barcoding techniques for avian influenza virus surveillance in migratory bird habitats. J Wildl Dis2010;46:64954DOIPubMed
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Cite This Article

DOI: 10.3201/eid2410.180461
Original Publication Date: 8/30/2018
1These authors contributed equally to this article.

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